반응식
C([NH:4][C:5]1[N:10]([OH:11])[C:9](=[NH:12])[N:8]=[C:7]([N:13]2[CH2:18][CH2:17][CH2:16][CH2:15][CH2:14]2)[CH:6]=1)(=O)C.[OH-].[Na+]>C(O)C>[NH2:4][C:5]1[N:10]([OH:11])[C:9](=[NH:12])[N:8]=[C:7]([N:13]2[CH2:14][CH2:15][CH2:16][CH2:17][CH2:18]2)[CH:6]=1참가 물질
4
실험 절차
0 5 g (2 mmoles) of 6-acetamido-1,2-dihydro-1-hydroxy-2-imino-4-piperidinopyrimidine prepared as described in Example 6 is dissolved in a mixture containing 10 ml of ethanol and 4 ml of 1N sodium hydroxide solution, the mixture is refluxed for 30 minutes, then evaporated under reduced pressure. After taking up the residue in 10 ml of water, the crystals are filtered, washed with water and dried to give the aimed compound in a yield of 0.35 g (85%), which shows no melting point depression when mixed with the product of Example 1.
후처리
- dissolutionis dissolved in a mixture
- temperaturethe mixture is refluxed for 30 minutes
- customevaporated under reduced pressure
- filtrationthe crystals are filtered
- washwashed with water
- customdried
출처 및 근거
- ORD 기록
- ord-8e86641f6b2c4d86a1e65c727d246f00
- 출처 데이터셋
- uspto-grants-1990_10
- 특허 번호
- US04960888
연결된 노트
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